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FDA 510(k)

SALTZMAN STETHOSCOPE HEAD

K-Number: K854771 · 1986-05-09

ApplicantK & S Medicorp
Decision Date1986-05-09
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SALTZMAN STETHOSCOPE HEAD is the device name listed in this FDA 510(k) record. The listed applicant is K & S Medicorp. It received FDA 510(k) clearance on 1986-05-09 under 510(k) number K854771. The device is classified under product code LDE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SALTZMAN STETHOSCOPE HEAD?

SALTZMAN STETHOSCOPE HEAD is a medical device that received FDA 510(k) clearance on 1986-05-09. The listed applicant is K & S Medicorp. The 510(k) number is K854771.

When did SALTZMAN STETHOSCOPE HEAD receive FDA 510(k) clearance?

SALTZMAN STETHOSCOPE HEAD received FDA 510(k) clearance on 1986-05-09, under 510(k) number K854771.

Who is the listed applicant for SALTZMAN STETHOSCOPE HEAD?

The FDA 510(k) record lists K & S Medicorp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SALTZMAN STETHOSCOPE HEAD?

The FDA product code for SALTZMAN STETHOSCOPE HEAD is LDE.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing K & S Medicorp as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K862131SALTZMAN EAR(TM) ENDOTRACHEAL ASCULTATION RECEPTORK854772TRANSCOR (TM) RADIO-STETHOSCOPE

Related Devices (Code: LDE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K945082CYPRESS MEDICAL PRODUCTS STETHOSCOPECypress Medical Products, Ltd.K944337VARIOUS STETHOSCOPESRud Riester GmbH & CO KGK940578MANUAL STETOSCOPEBhs Intl., Inc.K935944PROSCOPES AND ADSCOPESAmerican Diagnostic Corp.K923327STETHOSCOPE COVERAnup Chakraborty Co.K924095TIMEOSCOPE AND FLEXISCOPEStethoscopes of America, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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